epidermolysis bullosa

Preferred Label : epidermolysis bullosa;

MeSH definition : Group of genetically determined disorders characterized by the blistering of skin and mucosae. There are four major forms: acquired, simple, junctional, and dystrophic. Each of the latter three has several varieties.;

MeSH synonym : acantholysis bullosa;

MeSH annotation : vesiculobullous skin dis; GEN only: prefer specifics; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES; general or unspecified; prefer specifics;

Wikipedia link : https://en.wikipedia.org/wiki/Epidermolysis bullosa;

Details

Origin ID

D004820;

UMLS CUI

C0014527;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Dystrophic epidermolysis bullosa [ICD-11 Category]
- Epidermolysis bullosa simplex [ICD-10 Sub-category (who)]
- Epidermolysis bullosa simplex [ICD-11 Category]
- Inherited epidermolysis bullosa (disorder) [Inactive SNOMED CT concept]
- Junctional epidermolysis bullosa [ICD-11 Category]
- Other epidermolysis bullosa [ICD-10 Sub-category (who)]
Currated CISMeF NLP mapping
- Acquired epidermolysis bullosa [MedDRA Preferred Term]
- Epidermolysis Bullosa [NCIt concept]
- Epidermolysis bullosa [PASCAL descriptor]
- Epidermolysis bullosa [ICD-10 category]
- Epidermolysis bullosa [ICD-10 category (who)]
- Epidermolysis bullosa [MedDRA Preferred Term]
- Epidermolysis bullosa (disorder) [SNOMED CT concept]
- Epidermolysis bullosa, unspecified [ICD-10 Sub-category (who)]
- Epidermolysis bullosa, unspecified [ICD-10 Sub-category]
- Inherited epidermolysis bullosa [ORDO Disease]
- epidermolysis bullosa [DO Concept]
- epidermolysis bullosa [Disease (Nov.)]
- epidermolysis bullosa, nos [SNOMED Notion]
DO Cross reference
- epidermolysis bullosa [DO Concept]
Indexing information
- epidermolysis bullosa acquisita antigen [MeSH Supplementary Concept]
Manual NTBT mappings (CISMeF)
- Epidermal disease [ORDO Disease]
- Genetic epidermal disorder [ORDO Disease]
- Genodermatosis with ocular features [ORDO Disease]
- Kindler epidermolysis bullosa [ORDO Disease]
Record concept(s)
- epidermolysis bullosa [MeSH concept]
Related MeSH Supplementary Concept(s)
- bullous dystrophy, hereditary macular type [MeSH Supplementary Concept]
- epidermolysis bullosa pruriginosa [MeSH Supplementary Concept]
- epidermolysis bullosa with deficiency of galactosylhydroxylysyl glucosyltransferase [MeSH Supplementary Concept]
- epidermolysis bullosa with diaphragmatic hernia [MeSH Supplementary Concept]
- epidermolysis bullosa, lethal acantholytic [MeSH Supplementary Concept]
- nephropathy with pretibial epidermolysis bullosa and deafness [MeSH Supplementary Concept]
- poikiloderma of kindler [MeSH Supplementary Concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Epidermolysis Bullosa [NCIt concept]
- Epidermolysis bullosa [ICD-10 category (who)]
- Epidermolysis bullosa [ICD-10 category]
- Epidermolysis bullosa [MedDRA Preferred Term]
- Epidermolysis bullosa [PASCAL descriptor]
- Epidermolysis bullosa (disorder) [SNOMED CT concept]
- Epidermolysis bullosa, unspecified [ICD-10 Sub-category]
- Epidermolysis bullosa, unspecified [ICD-10 Sub-category (who)]
- epidermolysis bullosa [DO Concept]
- epidermolysis bullosa [Disease (Nov.)]
- epidermolysis bullosa, nos [SNOMED Notion]

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